PS Product Services GmbH
DE-MF-000005290 · Germany · Sankt Augustin
PS Product Services GmbH is registered in the European database on medical devices as a manufacturer, with 296 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 296 |
|---|
Most frequent device types declared: Verbände.
Devices declared under this manufacturer
- BARFUSS
- Curafit
- Dontodent
- Prokudent
- Tchibo
- Vitalis
- active MED
- activeMED
- activeMed
- curafit
- elkos
Showing 12 of 296 declared devices.
Catalogue references include FP0022, FP0023, SP0112, SP0120, SP0132, SP0154.
European nomenclature codes declared: M0399, V9099, M030499.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 296 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 296 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. PS Product Services GmbH was not found in either the U.S. or the Canadian register.